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- source_evidence_literature type ECO_0000212 NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_provenance.
- NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_assertion description "[Here, we describe two patients bearing translocation t(11;17) presenting with a clinical diagnosis of de novo myelodysplastic syndrome (MDS): the first with sole karyotypic abnormality 46,XY,t(11;17)(p11.2; p13) and the second where it represented one of the two karyotypic abnormalities 46,XX,del(5)(q13q33)46,XX,del(5)(q13q33),t(11;17)(q24;q23).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_provenance.
- NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_assertion evidence source_evidence_literature NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_provenance.
- NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_assertion SIO_000772 23147462 NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_provenance.
- NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_assertion wasDerivedFrom befree-20140225 NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_provenance.
- NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_assertion wasGeneratedBy ECO_0000203 NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP783071.RA0PaizAhq2xb4z13M3TZie_q2j1R9YPya2l1P9RNPx5I130_provenance.